Literature DB >> 30955892

Engineering a Model Cell for Rational Tuning of GPCR Signaling.

William M Shaw1, Hitoshi Yamauchi2, Jack Mead2, Glen-Oliver F Gowers1, David J Bell3, David Öling4, Niklas Larsson4, Mark Wigglesworth5, Graham Ladds6, Tom Ellis7.   

Abstract

G protein-coupled receptor (GPCR) signaling is the primary method eukaryotes use to respond to specific cues in their environment. However, the relationship between stimulus and response for each GPCR is difficult to predict due to diversity in natural signal transduction architecture and expression. Using genome engineering in yeast, we constructed an insulated, modular GPCR signal transduction system to study how the response to stimuli can be predictably tuned using synthetic tools. We delineated the contributions of a minimal set of key components via computational and experimental refactoring, identifying simple design principles for rationally tuning the dose response. Using five different GPCRs, we demonstrate how this enables cells and consortia to be engineered to respond to desired concentrations of peptides, metabolites, and hormones relevant to human health. This work enables rational tuning of cell sensing while providing a framework to guide reprogramming of GPCR-based signaling in other systems.
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  G protein-coupled receptor; Saccharomyces cerevisiae; biosensor; cell signaling; cell-to-cell communication; genome engineering; synthetic biology

Mesh:

Substances:

Year:  2019        PMID: 30955892      PMCID: PMC6476273          DOI: 10.1016/j.cell.2019.02.023

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  116 in total

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